510(k) K150030 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Fukuda Denshi DynaScope Model DS-8000 Series Patient Monitor
| Applicant | Fukuda Denshi USA, Inc., Redmond WA, US |
| Decision | Substantially Equivalent, Mar 16, 2015 |
| Received | Jan 8, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150030
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.